S9R (p.Ser9Arg) variant of IL1RN (P18510)
S9R (p.Ser9Arg) in IL1RN (P18510) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.04 / 1. The record also includes population frequency data and structural context.
S9R (p.Ser9Arg) variant details
- p.Ser9Arg
- 1000Genomes rs199841275
- ESP rs199841275
- ExAC rs199841275
- TOPMed rs199841275
- Missense
- Variant Prioritization Score for Impact Estimate 0.037
- REVEL 0.01
- CADD 2.95
- SIFT 0.22
- Most common in the African/African-American population (allele frequency 2.4e-05)
- Structural context available